Advanced 2 in 1 Hand Sanitizer

Manufacturer
THE SUN CO.LTD
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:02

Label at a glance#

ProductAdvanced 2 in 1 Hand Sanitizer
Active ingredientAlcohol
Label structure10 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease. ■ For use when soap and water are not available. ■ Recommended for repeated use.

Dosage and administration

■ Place enough product on hands to cover all surfaces. Rub hands together until dry. ■ For children under 6, use only under adult supervision ■ Avoid direct inhalation of vapors during application (Headaches and irritation to mucous membranes may occur when directly inhaled.) ■ This product is intended only for hand sanitizing. ■ To prevent drying out and contamination, close the lid completely after use. ■ Keep i...

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70.0%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Aminomethyl Propanol, Aloe Vera Gel, Grapefruit Seed Extract. Green Tea Extract, Butylene Glycol, Disodium EDTA, Phenoxyethanol

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat and flame.


Do not use ■ In children less than 2 months of age. ■ On open skin wounds


When using this product ■ Keep out of eyes, ears, and mouth ■ In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor
■ If irritation or rash occurs ■ These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If medical advice is needed, have the product container or label at hand.
■ If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.
■ For use when soap and water are not available.
■ Recommended for repeated use.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
■ For children under 6, use only under adult supervision
■ Avoid direct inhalation of vapors during application (Headaches and irritation to mucous membranes may occur when directly inhaled.)
■ This product is intended only for hand sanitizing.
■ To prevent drying out and contamination, close the lid completely after use.
■ Keep in their original container not to cause accidents nor diminish the integrity of the product.
■ Do not use over bandages, castings, etc. ad irritation may occur.

Other Information

OTHER SAFETY INFORMATION

Other Information

■ Store below 43°C (110°F)
■ May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74923-100-012022-01-28C16284748780-1d6a99b39-8def-a426-e053-dadaa90af4c27364a7e4-96c3-44a7-b099-e01d83cdaf69

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74923-100-01Advanced 2 in 1 Hand Sanitizer500 mL in 1 BOTTLE, PUMPGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74923-100ADVANCED 2 IN 1 HAND SANITIZER (ALCOHOL) GEL [THE SUN CO.LTD]2Legacy NDC, 1 package rows20200605_7364a7e4-96c3-44a7-b099-e01d83cdaf69.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74923-10074923-100-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
90b7c1af-b413-4e5b-8968-1398701e51017364a7e4-96c3-44a7-b099-e01d83cdaf692020-06-04WarningsExact identifier
spl id: 90b7c1af-b413-4e5b-8968-1398701e5101
spl set id: 7364a7e4-96c3-44a7-b099-e01d83cdaf69

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.